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立枯丝核菌AG 4HG-III引起南非马铃薯茎溃疡病的首次报道

First Report of Rhizoctonia solani AG 4HG-III Causing Potato Stem Canker in South Africa.

作者信息

Muzhinji N, Woodhall J W, Truter M, van der Waals J E

机构信息

Department of Microbiology and Plant Pathology, University of Pretoria, Private Bag X20, Hatfield, Pretoria 0028, South Africa, and Tobacco Research Board, Zimbabwe.

The Food and Environment Research Agency, Sand Hutton, York, Y041 1LZ, UK.

出版信息

Plant Dis. 2014 Jun;98(6):853. doi: 10.1094/PDIS-11-13-1131-PDN.

DOI:10.1094/PDIS-11-13-1131-PDN
PMID:30708692
Abstract

Black scurf and stem canker caused by Rhizoctonia solani Kühn (teleomorph: Thanathephorus cucumeris Frank Donk) are potato diseases of worldwide economic importance (4). R. solani consists of 13 anastomosis groups (AGs) of which AG 3-PT is considered the dominant causal agent of potato diseases globally (1,4). However, other AGs such as AG 2-1, 5, and 8 have been reported to cause potato diseases (1,4). In February 2013, potato stem samples (cv. Mondial) displaying dark brown lesions resembling those caused by Rhizoctonia stem canker were obtained from a commercial field in Limpopo Province, South Africa. Symptomatic tissue was disinfected with 1% NaOCl for 1 min, rinsed in sterile water, and 4-mm stem pieces excised from the margins of symptomatic tissues and plated on 2% water agar supplemented with 20 mg/l of chloramphenicol. Single hyphal tips taken from fungal isolates identified as R. solani based on morphological traits (3) were transferred to potato dextrose agar. DNA was isolated from the resulting cultures and ITS region of rDNA was sequenced as previously described (2). The resulting sequences of three of the isolates, Rh 81, Rh 82, and Rh 83 (KF712285, KF712286, and KF712287), were 99% similar to those of AG 4 HG-III found in GenBank (DQ102449 and AF354077). Therefore, based on molecular methods, these three isolates were identified as R. solani AG4 HG-III. To determine pathogenicity of the AG4 HG-III isolates, certified disease free mini-tubers (Generation 0, cv. Mondial, produced in tunnels) were used in pot trials. PDA plugs of each isolate were added to 10 g of barley grains, which had been sterilized by autoclaving for two consecutive days at 121°C for 30 min, and were incubated for 14 days until fully colonized. Ten colonized barley grains were placed 10 mm above each mini-tuber planted in 5l pots containing sterile potting mixture of sand:clay:pinebark (1:1:1). Ten tubers were inoculated with each isolate. Uninoculated, sterile barley grains were applied to the control treatment. Mini-tubers were grown in a greenhouse maintained at 22°C with light for a 12 h day. After 7 weeks, five plants for each isolate were destructively sampled and assessed for stem canker symptoms. At 120 days after sowing, the remaining five plants per treatment were assessed for blemishes on progeny tubers. The stem canker incidences of plants inoculated with Rh 81, Rh 82, and Rh 83 were 25, 25, and 50%, respectively, whereas no symptoms were observed in control plants. Sclerotia formation and blemishes were not observed on any of the progeny tubers, which might indicate that these strains are only able to infect stems, or that environmental conditions were not suitable for tuber blemish or black scurf development. R. solani AG4 HG-III was consistently re-isolated from symptomatic stems displaying brown lesions, and the identity of the re-isolates were confirmed by molecular tests as previously described, thereby fulfilling Koch's postulates. To our knowledge, this is the first report of R. solani AG4 HG-III causing stem canker on potato in South Africa and worldwide. Knowledge of which AGs are present in crop production systems is important when considering disease management strategies such as crop rotation and fungicide treatments (3). References: (1) C. Campion et al. Eur. J. Plant. Pathol. 109:983, 2003. (2) N. Muzhinji et al. Plant Dis. 98:570, 2014. (3) L. Tsror. J. Phytopathol. 158:649, 2010. (4) J. W. Woodhall et al. Plant. Pathol. 56:286, 2007.

摘要

由立枯丝核菌(有性型:瓜亡革菌)引起的黑痣病和茎溃疡病是对全球经济具有重要影响的马铃薯病害(4)。立枯丝核菌由13个融合群(AGs)组成,其中AG 3-PT被认为是全球马铃薯病害的主要致病因子(1,4)。然而,据报道其他AGs如AG 2-1、5和8也会引起马铃薯病害(1,4)。2013年2月,从南非林波波省的一个商业田地中采集了表现出深褐色病斑的马铃薯茎样本(品种为Mondial),这些病斑类似于由立枯丝核菌茎溃疡病引起的病斑。将有症状的组织用1%次氯酸钠消毒1分钟,在无菌水中冲洗,然后从有症状组织的边缘切下4毫米的茎段,接种在添加了20毫克/升氯霉素的2%水琼脂上。根据形态学特征(3)鉴定为立枯丝核菌的真菌分离物的单个菌丝尖端被转移到马铃薯葡萄糖琼脂上。从所得培养物中分离DNA,并按照先前描述的方法(2)对rDNA的ITS区域进行测序。分离物Rh 81、Rh 82和Rh 83(KF712285、KF712286和KF712287)的所得序列与GenBank中发现的AG 4 HG-III的序列相似度为99%。因此,基于分子方法,这三个分离物被鉴定为立枯丝核菌AG4 HG-III。为了确定AG4 HG-III分离物的致病性,在盆栽试验中使用了经认证无病的微型薯块(第0代,品种为Mondial,在隧道中生产)。将每个分离物的PDA菌块添加到10克经过连续两天在121°C下高压灭菌30分钟的大麦粒中,并培养14天直至完全定殖。将10个定殖的大麦粒放置在种植于装有无菌盆栽混合物(沙子:粘土:松树皮,1:1:1)的5升花盆中的每个微型薯块上方10毫米处。每个分离物接种10个微型薯块。将未接种的无菌大麦粒应用于对照处理。微型薯块在保持在22°C且光照为12小时/天的温室中生长。7周后,对每个分离物的五株植物进行破坏性采样,并评估茎溃疡症状。播种后120天,对每个处理剩余的五株植物评估后代薯块上的瑕疵。接种Rh 81、Rh 82和Rh 83的植物的茎溃疡发病率分别为25%、25%和50%,而对照植物未观察到症状。在任何后代薯块上均未观察到菌核形成和瑕疵,这可能表明这些菌株仅能感染茎,或者环境条件不适合薯块产生瑕疵或黑痣病发展。从表现出褐色病斑的有症状茎中持续重新分离到立枯丝核菌AG4 HG-III,并且如先前所述通过分子测试确认了重新分离物的身份,从而满足了柯赫氏法则。据我们所知,这是立枯丝核菌AG4 HG-III在南非和全球引起马铃薯茎溃疡病的首次报道。在考虑诸如轮作和杀菌剂处理等病害管理策略时,了解作物生产系统中存在哪些AGs很重要(3)。参考文献:(1)C. Campion等人,《欧洲植物病理学杂志》109:983,2003年。(2)N. Muzhinji等人,《植物病害》98:570,2014年。(3)L. Tsror,《植物病理学杂志》158:649,2010年。(4)J. W. Woodhall等人,《植物病理学》56:286,2007年。

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